Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.18 (A)
Location

Chromosome 1:209815925 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR084879

Most severe consequence
 
Regulatory region variant
Evidence status

Synonyms
HGVS name

1:g.209815925A>G

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 4032 sample genotypes, is associated with 1 phenotype and is mentioned in 31 citations.

Variant displays